Preclinical

In vitro assays help combat ectoparasite infections

Helping you develop new products

We offer a range of on and off-site preclinical services to help you develop new products.

We can help you define the formulation and safe dosage of your product, particularly in relation to pharmacokinetics, pharmacodynamics, toxicity and residue studies.

Pharmacokinetics

We provide a range of preclinical services from our GLP accredited laboratories to help with your research and development.

Our recent studies include:

  • Pharmacokinetics of anthelmintics in cattle
  • Bioequivalence of pour on anthelmintics in cattle

Tolerance

We can carry out tests to determine the safe dosage level for your new product as well as label extension activities for your existing products.

Our recent studies include:

  • Target animal safety bioequivalence and tissue residue studies
  • Target animal safety of in-feed coccidiostat in ducks and pheasants
  • Target animal safety of pour on anthelmintics in cattle
  • Safety and efficacy of the concurrent administration of vaccines in cattle
  • Safety of an overdose of a vaccine in pregnant and pre-breeding heifers
  • Field safety and anthelmintic efficacy of novel anthelmintic combo
  • Safety and efficacy of an anthelmintic combination pour-on against Fasciola hepatica and Cooperia oncophora in cattle
  • Safety and efficacy of in-feed anthelmintics against artificial infection Ascaris suum in fattening pigs
  • Safety and efficacy of in water benzimidazole against a naturally acquired infection of Ascaris suum
  • Safety and efficacy of the concurrent administration of PregSure BVD/Rispoval IBR-Marker vivum and PregSure BVD/Rispoval IBR Marker inactivatum in cattle

Residues

We provide on and off-site services from GLP accredited facilities.

Our recent studies include:

  • Tissue residue study of pour on anthelmintics in cattle
  • Target animal safety bioequivalence and tissue residue studies